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Identification of optimal sample collection devices and sampling locations for the detection of environmental viral contamination in wire poultry cages

Environmental testing of poultry premises after an outbreak of an infectious disease like avian influenza (AI) or Newcastle disease is essential to promptly verify virus‐free status and subsequently return to normal operations. In an attempt to establish an optimized sampling protocol, a laboratory...

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Autores principales: Mo, Jongseo, Spackman, Erica, Stephens, Christopher B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247023/
https://www.ncbi.nlm.nih.gov/pubmed/32643291
http://dx.doi.org/10.1111/tbed.13721
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author Mo, Jongseo
Spackman, Erica
Stephens, Christopher B.
author_facet Mo, Jongseo
Spackman, Erica
Stephens, Christopher B.
author_sort Mo, Jongseo
collection PubMed
description Environmental testing of poultry premises after an outbreak of an infectious disease like avian influenza (AI) or Newcastle disease is essential to promptly verify virus‐free status and subsequently return to normal operations. In an attempt to establish an optimized sampling protocol, a laboratory study simulating an AI virus‐contaminated poultry house with wire layer cages was conducted. Three sample collection devices, pre‐moistened cotton gauze, dry cotton gauze and a foam swab, were evaluated with each of four sample locations within a cage and when sampling all four locations with one device. Virus was detected with quantitative real‐time RT‐PCR utilizing a standard curve of a quantified homologous isolate of AI virus to determine titre equivalents of virus. The pre‐moistened gauze detected the most virus RNA (100% positive, geometric mean titre [GMT): 3.2 log(10) 50% embryo infectious doses [EID(50)] equivalents per 25 cm(2)) in all four sample locations compared to dry gauze (93% positive, GMT: 2.6 EID(50) equivalents per 25 cm(2)) and foam swabs (95% positive, GMT: 2.8 log10 EID(50) equivalents per 25 cm(2)). The highest viral RNA loads were observed from the cage floor, and when the four locations were sampled with the same device. Overall, the pre‐moistened gauze performed the best, and sampling multiple locations within a cage with the same device would likely optimize detection of residual virus.
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spelling pubmed-82470232021-07-02 Identification of optimal sample collection devices and sampling locations for the detection of environmental viral contamination in wire poultry cages Mo, Jongseo Spackman, Erica Stephens, Christopher B. Transbound Emerg Dis Original Articles Environmental testing of poultry premises after an outbreak of an infectious disease like avian influenza (AI) or Newcastle disease is essential to promptly verify virus‐free status and subsequently return to normal operations. In an attempt to establish an optimized sampling protocol, a laboratory study simulating an AI virus‐contaminated poultry house with wire layer cages was conducted. Three sample collection devices, pre‐moistened cotton gauze, dry cotton gauze and a foam swab, were evaluated with each of four sample locations within a cage and when sampling all four locations with one device. Virus was detected with quantitative real‐time RT‐PCR utilizing a standard curve of a quantified homologous isolate of AI virus to determine titre equivalents of virus. The pre‐moistened gauze detected the most virus RNA (100% positive, geometric mean titre [GMT): 3.2 log(10) 50% embryo infectious doses [EID(50)] equivalents per 25 cm(2)) in all four sample locations compared to dry gauze (93% positive, GMT: 2.6 EID(50) equivalents per 25 cm(2)) and foam swabs (95% positive, GMT: 2.8 log10 EID(50) equivalents per 25 cm(2)). The highest viral RNA loads were observed from the cage floor, and when the four locations were sampled with the same device. Overall, the pre‐moistened gauze performed the best, and sampling multiple locations within a cage with the same device would likely optimize detection of residual virus. John Wiley and Sons Inc. 2020-07-22 2021-03 /pmc/articles/PMC8247023/ /pubmed/32643291 http://dx.doi.org/10.1111/tbed.13721 Text en Published 2020. This article is a U.S. Government work and is in the public domain in the USA. Transboundary and Emerging Diseases published by Blackwell Verlag GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Mo, Jongseo
Spackman, Erica
Stephens, Christopher B.
Identification of optimal sample collection devices and sampling locations for the detection of environmental viral contamination in wire poultry cages
title Identification of optimal sample collection devices and sampling locations for the detection of environmental viral contamination in wire poultry cages
title_full Identification of optimal sample collection devices and sampling locations for the detection of environmental viral contamination in wire poultry cages
title_fullStr Identification of optimal sample collection devices and sampling locations for the detection of environmental viral contamination in wire poultry cages
title_full_unstemmed Identification of optimal sample collection devices and sampling locations for the detection of environmental viral contamination in wire poultry cages
title_short Identification of optimal sample collection devices and sampling locations for the detection of environmental viral contamination in wire poultry cages
title_sort identification of optimal sample collection devices and sampling locations for the detection of environmental viral contamination in wire poultry cages
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247023/
https://www.ncbi.nlm.nih.gov/pubmed/32643291
http://dx.doi.org/10.1111/tbed.13721
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